TY - JOUR
T1 - The Dmca1D channel mediates Ca2+ inward currents in Drosophila embryonic muscles
AU - Hara, Yusuke
AU - Koganezawa, Masayuki
AU - Yamamoto, Daisuke
N1 - Funding Information:
We thank M. Yoshihara for technical supervision on the electrophysiological experiments, M. Suyama for secretarial assistance, and the Bloomington Stock Center and the Drosophila Genetic Resource Center for fly stocks. This work was supported in part by Grants-in-Aid for Scientific Research (26113702, 26114502, 24113502, and 23220007 to D.Y., and 24570082 and 23115702 to M.K.) from the Japanese Government Ministry of Education, Culture, Sports, Science and Technology (MEXT) to D.Y., the Japan-France Bilateral Joint Research Project Grant from Japan Society for the Promotion of Science (JSPS) to D.Y., a Life Science Grant from the Takeda Science Foundation to D.Y., and a Grant-in-Aid for JSPS fellows (14J07885) to Y.H.
Publisher Copyright:
© 2015 Informa Healthcare USA, Inc.
PY - 2015/7/3
Y1 - 2015/7/3
N2 - We studied, in a genetic model organism, Drosophila melanogaster, the channel mechanisms underlying membrane excitation in the embryonic body wall muscle whose biophysical properties have been poorly characterized. The inward current underlying the action potential was solely mediated by a high-threshold class of voltage-gated Ca2+ channels, which exhibited slow inactivation, Ca2+ permeability with saturation at high [Ca2+]OUT, and sensitivity to a Ca2+ channel blocker, Cd2+. The Ca2+ current in the embryonic muscle was completely eliminated in Dmca1D mutants, indicating that the Dmca1D-encoded Ca2+ channel is the major mediator of inward currents in the body wall muscles throughout the embryonic and larval stages.
AB - We studied, in a genetic model organism, Drosophila melanogaster, the channel mechanisms underlying membrane excitation in the embryonic body wall muscle whose biophysical properties have been poorly characterized. The inward current underlying the action potential was solely mediated by a high-threshold class of voltage-gated Ca2+ channels, which exhibited slow inactivation, Ca2+ permeability with saturation at high [Ca2+]OUT, and sensitivity to a Ca2+ channel blocker, Cd2+. The Ca2+ current in the embryonic muscle was completely eliminated in Dmca1D mutants, indicating that the Dmca1D-encoded Ca2+ channel is the major mediator of inward currents in the body wall muscles throughout the embryonic and larval stages.
KW - Ca channel gating
KW - Capermeability
KW - mutants
KW - skeletal muscle
KW - whole-cell patch clamp relation
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U2 - 10.3109/01677063.2015.1054991
DO - 10.3109/01677063.2015.1054991
M3 - Article
C2 - 26004544
AN - SCOPUS:84946563247
SN - 0167-7063
VL - 29
SP - 117
EP - 123
JO - Journal of Neurogenetics
JF - Journal of Neurogenetics
IS - 2-3
ER -